Hydrogen sulfide increases glutathione production and suppresses oxidative stress in mitochondria von Kimura, Yuka, Goto, Yu-Ichi, Kimura, Hideo

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Concise Review: Heteroplasmic Mitochondrial DNA Mutations and Mitochondrial Diseases: Toward iPSC‐Based Disease Modeling, Drug Discovery, and Regenerative Therapeutics von Hatakeyama, Hideyuki, Goto, Yu‐ichi

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Estimation of the Number of Patients With Mitochondrial Diseases: A Descriptive Study Using a Nationwide Database in Japan von Ibayashi, Koki, Fujino, Yoshihisa, Mimaki, Masakazu, Fujimoto, Kenji, Matsuda, Shinya, Goto, Yu-ichi

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Mitochondrial Lon protease regulates mitochondrial DNA copy number and transcription by selective degradation of mitochondrial transcription factor A (TFAM) von Matsushima, Yuichi, Goto, Yu-ichi, Kaguni, Laurie S., Lehman, I. Robert

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CO2-sensitive tRNA modification associated with human mitochondrial disease von Lin, Huan, Miyauchi, Kenjyo, Harada, Tai, Okita, Ryo, Takeshita, Eri, Komaki, Hirofumi, Fujioka, Kaoru, Yagasaki, Hideki, Goto, Yu-ichi, Yanaka, Kaori, Nakagawa, Shinichi, Sakaguchi, Yuriko, Suzuki, Tsutomu

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Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice von Morinaga, Hidetaka, Kato, Hiroki, Otera, Hidenori, Nomura, Masatoshi, Maeda, Maki, Mihara, Katsuyoshi, Taguchi, Naoko, Goto, Yu-ichi, Nonaka, Ikuya, Suzuki, Satoshi O, Masuda, Keiji, Jofuku, Akihiro, Ishihara, Naotada, Takayanagi, Ryoichi, Yokota, Sadaki, Nakanishi, Yae

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ECHS1 Mutations Cause Combined Respiratory Chain Deficiency Resulting in Leigh Syndrome von Sakai, Chika, Yamaguchi, Seiji, Sasaki, Masayuki, Miyamoto, Yusaku, Matsushima, Yuichi, Goto, Yu-ichi

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COX6A2 variants cause a muscle‐specific cytochrome c oxidase deficiency von Inoue, Michio, Uchino, Shumpei, Iida, Aritoshi, Noguchi, Satoru, Hayashi, Shinichiro, Takahashi, Tsutomu, Fujii, Katsunori, Komaki, Hirofumi, Takeshita, Eri, Nonaka, Ikuya, Okada, Yukinori, Yoshizawa, Takuya, Van Lommel, Leentje, Schuit, Frans, Goto, Yu‐ichi, Mimaki, Masakazu, Nishino, Ichizo

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Investigating DNA Methylation of SHATI/NAT8L Promoter Sites in Blood of Unmedicated Patients with Major Depressive Disorder von Miyanishi, Hajime, Uno, Kyosuke, Iwata, Mina, Kikuchi, Yuu, Yamamori, Hidenaga, Yasuda, Yuka, Ohi, Kazutaka, Hashimoto, Ryota, Hattori, Kotaro, Yoshida, Sumiko, Goto, Yu-ichi, Sumiyoshi, Tomiki, Nitta, Atsumi

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Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy von Bonora, Elena, Chakrabarty, Sanjiban, Kellaris, Georgios, Tsutsumi, Makiko, Bianco, Francesca, Bergamini, Christian, Ullah, Farid, Isidori, Federica, Liparulo, Irene, Diquigiovanni, Chiara, Masin, Luca, Rizzardi, Nicola, Cratere, Mariapia Giuditta, Boschetti, Elisa, Papa, Valentina, Maresca, Alessandra, Cenacchi, Giovanna, Casadio, Rita, Martelli, Pierluigi, Matera, Ivana, Ceccherini, Isabella, Fato, Romana, Raiola, Giuseppe, Arrigo, Serena, Signa, Sara, Sementa, Angela Rita, Severino, Mariasavina, Striano, Pasquale, Fiorillo, Chiara, Goto, Tsuyoshi, Uchino, Shumpei, Oyazato, Yoshinobu, Nakamura, Hisayoshi, Mishra, Sushil K., Yeh, Yu-Sheng, Kato, Takema, Nozu, Kandai, Tanboon, Jantima, Morioka, Ichiro, Nishino, Ichizo, Toda, Tatsushi, Goto, Yu-ichi, Ohtake, Akira, Kosaki, Kenjiro, Yamaguchi, Yoshiki, Nonaka, Ikuya, Iijima, Kazumoto, Mimaki, Masakazu, Kurahashi, Hiroki, Raams, Anja, MacInnes, Alyson, Alders, Mariel, Engelen, Marc, Linthorst, Gabor, de Koning, Tom, den Dunnen, Wilfred, Dijkstra, Gerard, van Spaendonck, Karin, van Gent, Dik C., Aronica, Eleonora M., Picco, Paolo, Carelli, Valerio, Seri, Marco, Katsanis, Nicholas, Duijkers, Floor A. M., Taniguchi-Ikeda, Mariko, De Giorgio, Roberto

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Insulin-Like Growth Factor Binding Protein-3 Deficiency Leads to Behavior Impairment with Monoaminergic and Synaptic Dysfunction von Dai, Hongmei, Goto, Yu-ichi, Itoh, Masayuki

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Plasma Metabolites Predict Severity of Depression and Suicidal Ideation in Psychiatric Patients-A Multicenter Pilot Analysis von Setoyama, Daiki, Kato, Takahiro A, Hashimoto, Ryota, Kunugi, Hiroshi, Hattori, Kotaro, Hayakawa, Kohei, Sato-Kasai, Mina, Shimokawa, Norihiro, Kaneko, Sachie, Yoshida, Sumiko, Goto, Yu-Ichi, Yasuda, Yuka, Yamamori, Hidenaga, Ohgidani, Masahiro, Sagata, Noriaki, Miura, Daisuke, Kang, Dongchon, Kanba, Shigenobu

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Whole genome sequencing of 45 Japanese patients with intellectual disability von Abe‐Hatano, Chihiro, Iida, Aritoshi, Kosugi, Shunichi, Momozawa, Yukihide, Terao, Chikashi, Ishikawa, Keiko, Okubo, Mariko, Hachiya, Yasuo, Nishida, Hiroya, Nakamura, Kazuyuki, Miyata, Rie, Murakami, Chie, Takahashi, Kan, Hoshino, Kyoko, Sakamoto, Haruko, Ohta, Sayaka, Kubota, Masaya, Takeshita, Eri, Ishiyama, Akihiko, Nakagawa, Eiji, Sasaki, Masayuki, Kato, Mitsuhiro, Matsumoto, Naomichi, Kamatani, Yoichiro, Kubo, Michiaki, Takahashi, Yoshiyuki, Natsume, Jun, Inoue, Ken, Goto, Yu‐Ichi

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Myoclonic Epilepsy with Ragged-red Fibers with Intranuclear Inclusions von Kawazoe, Tomoya, Tobisawa, Shinsuke, Sugaya, Keizo, Uruha, Akinori, Miyamoto, Kazuhito, Komori, Takashi, Goto, Yu-ichi, Nishino, Ichizo, Yoshihashi, Hiroshi, Mizuguchi, Takeshi, Matsumoto, Naomichi, Egawa, Naohiro, Kawata, Akihiro, Isozaki, Eiji

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5-HT1A Receptor Agonist Treatment Partially Ameliorates Rett Syndrome Phenotypes in mecp2-Null Mice by Rescuing Impairment of Neuron Transmission and the CREB/BDNF Signaling Pathwa... von Dai, Hongmei, Kitami, Yoshikazu, Goto, Yu-ichi, Itoh, Masayuki

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DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion i... von Terasaki, Akane, Nakamura, Masayuki, Urata, Yuka, Hiwatashi, Hanae, Yokoyama, Izumi, Yasuda, Takeshi, Onuma, Teiichi, Wada, Kazumaru, Kaneko, Sunao, Kan, Rumiko, Niwa, Shin-Ichi, Hashimoto, Ohiko, Komure, Osamu, Goto, Yu-Ichi, Yamagishi, Yuko, Nakano, Misa, Furusawa, Yoshihiko, Sano, Akira

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Mitochondrial respiratory dysfunction caused by a heteroplasmic mitochondrial DNA mutation blocks cellular reprogramming von Yokota, Mutsumi, Hatakeyama, Hideyuki, Okabe, Saki, Ono, Yasuha, Goto, Yu-ichi

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Nervonic acid level in cerebrospinal fluid is a candidate biomarker for depressive and manic symptoms: A pilot study von Kageyama, Yuki, Deguchi, Yasuhiko, Hattori, Kotaro, Yoshida, Sumiko, Goto, Yu‐ichi, Inoue, Koki, Kato, Tadafumi

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National Center Biobank Network von Omae, Yosuke, Goto, Yu-ichi, Tokunaga, Katsushi

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Respiratory Chain Complex Disorganization Impairs Mitochondrial and Cellular Integrity: Phenotypic Variation in Cytochrome c Oxidase Deficiency von Hatakeyama, Hideyuki, Goto, Yu-Ichi

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